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- W137738862 endingPage "270" @default.
- W137738862 startingPage "207" @default.
- W137738862 abstract "Safe and efficacious gene delivery requires a suitable vector. The role of viral vectors in gene delivery is primary due to their function in the delivery of genetic material into host cells. However, the major problem in the use of viral vectors in gene therapy is immunogenic reaction risks and short-lived expression, which is of utmost importance to researchers. The continuous efforts to develop well-refined viral vector-mediated gene delivery protocols have raised the hope of a convenient, safe, stable, and reproducible transduction of functional genetic material into specific cells. Viral vectors are advantageous for targeting and efficiently entering cells as they can be modified according to the required application. Adenovirus (Ad) vectors, adeno-associated virus (AAV) vectors, retrovirus vectors, and herpesvirus vectors are the few viral vectors that have advanced to clinical trials aimed at developing gene therapy products for their safety and biological function. Viral vectors like baculovirus, lentivirus, influenza viruses, human papillomaviruses (HPV), and hepatitis B virus (HBV) can also be reported as gene delivery vehicles in the treatment of various human colorectal carcinomas, diabetes, avian influenza, cancer of the cervix, and liver diseases." @default.
- W137738862 created "2016-06-24" @default.
- W137738862 creator A5030417466 @default.
- W137738862 creator A5066256925 @default.
- W137738862 date "2011-01-01" @default.
- W137738862 modified "2023-09-25" @default.
- W137738862 title "Gene Delivery Using Viral Vectors" @default.
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